What made Trestolone acetate unique among experimental androgens was its C-7 methylation, which blocked aromatization and DHT conversion. This rare configuration allowed the compound to act as a pure androgen with minimized estrogenic and prostatic side effects. Additionally, its inability to bind to sex hormone-binding globulin meant higher bioavailability and greater potency than testosterone. These characteristics made it a top candidate for experimental therapies aimed at mimicking natural testosterone benefits without its unwanted conversions or fluctuations in serum levels.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
Disclaimer: Information provided it this page is for general information only and does not substitute for professional medical advice.
For detailed information about MENT TREST 50 by Aaster Solutions, consult with your doctor or healthcare professional.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.
Llewellyn, W. (2017). William Llewellyn's Anabolics.
United States: Molecular Nutrition, LLC.